Mobility and Reactivity of Cu+ Species in Cu-CHA Catalysts under NH3-SCR-NOx Reaction Conditions: Insights from AIMD Simulations
| Autor: | Millan, Reisel, Cnudde, Pieter, van Speybroeck, Veronique, Boronat, Mercedes |
|---|---|
| Přispěvatelé: | Ministerio de Economía y Competitividad (España), European Commission |
| Rok vydání: | 2021 |
| Předmět: |
Cation mobility
Reaction mechanism Chabazite Technology and Engineering MIGRATION Diffusion SPECTROSCOPIC EVIDENCE mechanism chemistry.chemical_element Molecular dynamics 010402 general chemistry DFT 01 natural sciences Article cation mobility Catalysis CU-SSZ-13 NOX CONVERSION PROFILE Reactivity (chemistry) zeolite QD1-999 NOx SITES Zeolite ZEOLITES 010405 organic chemistry Chemistry Selective catalytic reduction Copper molecular dynamics 0104 chemical sciences 3. Good health DYNAMIC NATURE REDUCTION Physics and Astronomy 13. Climate action COPPER IONS Physical chemistry Mechanism |
| Zdroj: | JACS AU JACS Au, Vol 1, Iss 10, Pp 1778-1787 (2021) JACS Au Digital.CSIC. Repositorio Institucional del CSIC instname |
| ISSN: | 2691-3704 |
| DOI: | 10.1021/jacsau.1c00337 |
| Popis: | The mobility of the copper cations acting as active sites for the selective catalytic reduction of nitrogen oxides with ammonia in Cu-CHA catalysts varies with temperature and feed composition. Herein, the migration of [Cu(NH3)2]+ complexes between two adjacent cavities of the chabazite structure, including other reactant molecules (NO, O2, H2O, and NH3), in the initial and final cavities is investigated using ab initio molecular dynamics (AIMD) simulations combined with enhanced sampling techniques to describe hopping events from one cage to the other. We find that such diffusion is only significantly hindered by the presence of excess NH3 or NO in the initial cavity, since both reactants form with [Cu(NH3)2]+ stable intermediates which are too bulky to cross the 8-ring windows connecting the cavities. The presence of O2 modifies strongly the interaction of NO with Cu+. At low temperatures, we observe NO detachment from Cu+ and increased mobility of the [Cu(NH3)2]+ complex, while at high temperatures, NO reacts spontaneously with O2 to form NO2. The present simulations give evidence for recent experimental observations, namely, an NH3 inhibition effect on the SCR reaction at low temperatures, and transport limitations of NO and NH3 at high temperatures. Our first principle simulations mimicking operating conditions support the existence of two different reaction mechanisms operating at low and high temperatures, the former involving dimeric Cu(NH3)2-O2-Cu(NH3)2 species and the latter occurring by direct NO oxidation to NO2 in one single cavity. This work has been supported by the Spanish Government through Severo Ochoa (SEV-2016-0683, MINECO), and MAT2017-82288-C2-1-P (AEI/FEDER, UE) projects, and by CSIC through the i-link+ program (LINKA20381). We thankfully acknowledge Red Española de Supercomputación (RES) and Servei d’Informàtica de la Universitat de València (SIUV) for computational resources and technical support, the computer resources at Marenostrum4 (RES-QS-2020-1-0029 and RES-QS.2020-2-0015) and the technical support provided by BSC. R.M. thanks ITQ for his contract. V.V.S, P.C. acknowledge funding from the European Union’s Horizon 2020 research and innovation program (consolidator ERC grant agreement No. 647755 - DYNPOR (2015-2020)). V.V.S. acknowledges the Research Board of the Ghent University (BOF). Part of the computational resources and services used were provided by Ghent University (Stevin Supercomputer Infrastructure), the VSC (Flemish Supercomputer Center), funded by the Research Foundation - Flanders (FWO). |
| Databáze: | OpenAIRE |
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